1606-80-0 Usage
Description
AllylSulfonicAcid, also known as 2-Propen-1-sulfonic acid, is a colorless to pale yellow liquid with a pungent odor. It is a strong acid and is widely used in various industrial applications.
Used in Polymer Production:
AllylSulfonicAcid is used as a monomer for the production of polymers, contributing to the formation of polymer chains and enhancing their properties.
Used in Ion Exchange Resin Synthesis:
AllylSulfonicAcid is used as a co-monomer in the synthesis of ion exchange resins, improving their functional groups and ion-exchange capabilities.
Used in Metal Plating Processes:
AllylSulfonicAcid is used as a corrosion inhibitor in metal plating processes, protecting metal surfaces from corrosion and enhancing the quality of the plated layers.
Used as a Catalyst in Chemical Reactions:
AllylSulfonicAcid is used as a catalyst to accelerate chemical reactions, improving reaction rates and yields.
Used in Vinyl Polymer Production:
AllylSulfonicAcid is used as a stabilizer in the production of vinyl polymers, ensuring the stability and quality of the final product.
Used in Specialty Chemicals and Pharmaceuticals:
AllylSulfonicAcid is utilized in the production of specialty chemicals and pharmaceuticals, contributing to the synthesis and properties of various compounds.
Note: Due to its corrosive and toxic nature, proper handling and storage of AllylSulfonicAcid are necessary to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 1606-80-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1606-80:
(6*1)+(5*6)+(4*0)+(3*6)+(2*8)+(1*0)=70
70 % 10 = 0
So 1606-80-0 is a valid CAS Registry Number.
1606-80-0Relevant articles and documents
Millburn,Venanzi
, p. 97,98, 100 (1968)
A general and efficient method for the preparation of organic sulfonic acids by insertion of sulfur trioxide into the metal-carbon bond of organolithiums
Smith, Keith,Hou, Duanjie
, p. 1530 - 1532 (2007/10/03)
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MECHANISTIC VARIATION IN ALKANESULFONYL CHLORIDE HYDROLYSIS AND RELATED REACTIONS
King, J. F.,Lam, J. Y. L.,Skonieczny, S.
, p. 177 - 180 (2007/10/02)
Kinetic and product ratio studies are consistent with the following mechanisms for the hydrolysis of methanesulfonyl chloride: (a) in acidic medium (pH 1-6) via a direct substitution on sulfur (SN2-S), (b) in mildly basic medium (pH 8-10) by way of sulfene (CH2=SO2) formation followed by trapping with water, and (c) in strongly basic solution (pH >10) via sulfene with trapping by the hydroxide ion.The reactions of primary and secondary alkanesulfonyl chlorides are qualitatively similar.
